Radiation-induced expression of functional Fas ligand in EBV-positive human nasopharyngeal carcinoma cells

Int J Cancer. 2000 Apr 15;86(2):229-37. doi: 10.1002/(sici)1097-0215(20000415)86:2<229::aid-ijc12>3.0.co;2-1.

Abstract

Ionizing radiation remains a major therapeutic tool against human cancers, especially epithelial tumors, which account for the majority of human malignancies. Although Fas and Fas-L are essential determinants of apoptosis, few data support their role in the cytotoxic effect of ionizing radiation. Epstein-Barr-virus (EBV)-positive nasopharyngeal carcinoma (NPC) were chosen to address this question owing to their known sensitivity to ionizing radiation and their constitutive expression of the Fas-receptor. We here report that, in xenografted NPC cells, Fas-L expression, which was very low in basal conditions, was dramatically increased by tumor irradiation. Both the Fas receptor and the Fas ligand were found to be functional in this model, and a high proportion of irradiated NPC cells underwent apoptosis following tumor irradiation. Induction of Fas-L expression and apoptosis were observed for doses as low as 2 Gy. These data show an increase in Fas-L expression upon irradiation exposure, and strongly suggest that, in some epithelial malignancies, Fas-mediated apoptosis can play a major role in the anti-tumor effect of ionizing radiation, in the range of doses used for therapeutic applications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Cell Membrane / chemistry
  • Dose-Response Relationship, Radiation
  • Fas Ligand Protein
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Herpesvirus 4, Human / isolation & purification*
  • Humans
  • Jurkat Cells / pathology
  • Kinetics
  • Membrane Glycoproteins / analysis
  • Membrane Glycoproteins / biosynthesis*
  • Mice
  • Mice, Nude
  • Microscopy, Confocal
  • Nasopharyngeal Neoplasms / metabolism
  • Nasopharyngeal Neoplasms / radiotherapy*
  • Nasopharyngeal Neoplasms / virology
  • Neoplasm Transplantation
  • Transplantation, Heterologous
  • fas Receptor / analysis
  • fas Receptor / biosynthesis*

Substances

  • FASLG protein, human
  • Fas Ligand Protein
  • Fasl protein, mouse
  • Membrane Glycoproteins
  • fas Receptor